Phosphorescent meso-unsubstituted metallo-porphyrin probe molecules for measuring oxygen and imaging methods

ABSTRACT

Oxygen levels in biological tissue or systems can be measured by the phosphorescence quenching method using phosphorescent porphyrin probes, also referred to as a dendritic oxygen probes, with controllable quenching parameters and defined biodistributions. Provided are a “next generation” of oxygen sensors with substantially improved phosphorescence emission for better imaging capabilities, ease of use, increasing the quantum efficiency (phosphorescence intensity) and extending their range of applicability including constructing a class of oxygen sensors for making measurements in organic media. In addition, provided are methods for synthesizing new porphyrin constructs in which the porphyrin is made less flexible and more planar, changing with decrease internal quenching, and thereby increasing the phosphorescence emission used for oxygen sensing. Additional methods are provided for structurally modifying the dendrimer used to encapsulate the porphyrin phosphor to provide internal quenching of singlet oxygen molecules formed during oxygen measurements.

CROSS-REFERENCE TO RELATED APPLICATIONS

The present invention is a continuation-in-part of, and claims priority to, U.S. Non-Provisional patent application Ser. No. 13/778,777, filed on Feb. 27, 2013, issued as U.S. Pat. No. 9,556,213 on Jan. 31, 2017, which, in turn, claimed priority to U.S. Provisional Application Ser. No. 61/603,668, filed on Feb. 27, 2012, both of which are incorporated herein in their entirety.

GOVERNMENT INTEREST

This invention was supported in part by funds from the U.S. Government (National Institutes of Health) Grant No. HL0812273, R01EB007279, EB018464, and NS092986, and the U.S. Government may therefore have certain rights in the invention.

FIELD OF THE INVENTION

The present invention relates to highly accurate and versatile optical method for oxygen measurement, particularly useful for applications in living human and animal tissue, and more particularly to novel phosphorescent probe molecules that possess brighter signal, well-defined chemical composition, and can potentially be used in clinics.

BACKGROUND OF THE INVENTION

The reliable and accurate measurement of oxygen supply in mammalian tissue is important to ensure that the oxygen supply is adequate. The circulatory system employs special oxygen-carrying protein molecules in red blood cells (hemoglobin) to deliver oxygen from the lungs throughout the body. Once dissociated from hemoglobin, oxygen is delivered to its consumption sites in cells by diffusion. It is the measurement of this dissolved unbound oxygen that is most critical for quantifying tissue physiological status. The phosphorescence quenching method underpinning this patent application is unique in its ability to accomplish such a measurement. This method is based on use of special phosphorescent probe molecules, which report on oxygen concentration in the environment with high specificity and accuracy.

Measurements of oxygen by phosphorescence quenching provide information on oxygen consumption by the tissue, and through that, allow evaluation of tissue diseased states. Oxygen is a key metabolite, and tissue hypoxia is a critical parameter with respect to various tissue pathologies, such as retinal diseases (Berkowitz et al., Invest. Ophthalmol. Visual Sci. 40:2100-2105 (1999); Linsenmeier et al., Ophthalmol. Visual Sci. 39:1647-1657 (1998)), brain abnormalities (Vannucci et al., J. Exp. Biol. 207:3149-3154 (2004); Brunel et al., J. Neuroradiology 31:123-137 (2004); Johnston et al., Neuroscientist 8:212-220 (2002)), and cancer (Evans et al., J. Appl. Physiol. 98:1503-1510 (2005)). Different oxygen levels in tissues can be indicative of tissue structure abnormalities, defects, whether caused externally, or by genetic manifestations, resulting from disease.

Imaging tissue oxygen in vivo presents a challenging and important problem. Nevertheless, currently developing imaging technologies for mapping tissue oxygenation (Rajendran et al., Radiol. Clin. North Am. 43:169-187 (2005)) (e.g., NMR/EPR (Subramanian et al. NMR Biomed. 17:263-294 (2004)), PET (Piert et al., Nucl. Med. 46:106-113 (2005); Apisarnthanarax et al., Rad. Res. 163:1-25 (2005)), near infrared tomographic techniques (Fenton et al., Brit. J. Cancer 79:464-471 (1999); Liu et al., Appl. Opt. 39:5231-5243 (2000)), etc (Ballinger, Sem. Nucl. Med. 31:321-329 (2001); Foo et al., Mol. Imag. Biol. 6:291-305 (2004)) suffer from many deficiencies, including invasiveness, low spatial and/or temporal resolution, lack of absolute calibration, poor specificity, etc., and remain yet to be adequately developed.

The phosphorescence quenching method (Vanderkooi et al., J. Biol. Chem. 262:5476-5483 (1987); Wilson & Vinogradov, In: Handbook of Biomedical Fluorescence. Mycek M-A, Pogue B W, eds. Marcel Dekker; New York: 2003. Ch. 17) is superior in its ability to directly detect oxygen in tissue. A detailed summary is presented by Vinogradov & Wilson (2012) “Porphyrin-dendrimers as biological oxygen sensors,” In Designing Dendrimers (Capagna, Ceroni, Eds.), Wiley, New York) following the effective filing date of this invention. When a phosphorescent probe is dissolved in the blood and excited using appropriate illumination, its phosphorescence lifetime and intensity become robust indicators of oxygen concentration in the environment. Phosphorescence quenching is exquisitely sensitive and selective to oxygen, possesses excellent temporal resolution and can be implemented for high-resolution hypoxia imaging in 2D (Rumsey et al., Science. 241:1649-1652 (1988); Vinogradov et al., Biophys. J. 70:1609-1617 (1996); Shonat et al., Annal. Biomed. Eng. 31:1084-1096 (2003)).

Efforts to develop 3D near infrared tomographic modality for mapping tissue oxygenation using phosphorescences, include Soloviev et al., Applied Optics 42:113 (2003); Soloviev et al., Applied Optics 43:564 (2004); Apreleva et al., Optics Letters 31:1082 (2006); Apreleva et al., Applied Optics 45:8547 (2006); Apreleva et al., Optics Letters 33:782 (2008), and recent clinically relevant developments of Cerenkov radiation-induced phosphorescence (Zhang et al., Biomedical Optics Express 3:2381 (2012). But highly accurate and versatile methods for measuring oxygen remain to be further developed.

For phosphorescent compounds to be suitable for use as a phosphorescent oxygen probe (aka “phosphor” or “oxyphor”) in determination of tissue oxygenation, it is desirable that the compounds have (1) high absorbance in the near infrared region of the spectrum where natural chromophores of tissue, such as hemoglobin or myoglobin, have only very weak absorption; (2) phosphorescence with high quantum yields at room temperature, preferably greater than 0.05; and (3) suitable lifetimes, preferably from about 0.3 to about 1 msec.

A new class of phosphors suitable for oxygen measurement was previously reported in Vinogradov and Wilson, J. Chem. Soc., Perkin Trans. 2, 103-111 (1995), and in U.S. Pat. No. 4,947,850, “Method and Apparatus for Imaging an Internal Body Portion of a Host Animal,” by Vanderkooi and Wilson), and U.S. Pat. No. 5,837,865, “Phosphorescent Dendritic Macromolecular Compounds for Imaging Tissue Oxygen,” by Vinogradov and Wilson), which are incorporated herein by reference. In the general, the phosphorescent probes for oxygen measurements comprise three functional parts: 1) phosphorescent core; 2) encapsulating and protecting ligands and 3) the hydrophilic outer layer, which is usually made of monomethyloligoethyleneglycol or simply polyethyleneglycol (PEG) residues. Parts 2 and 3 comprise the so-called immediate “surrounding environment” of the phosphorescent core chromophore.

The functions of the three parts are as follows: a) phosphorescent core provides optical signal (phosphorescence), inducible by red/near infrared excitation sources and responsive to changes in the partial pressure of oxygen (pO₂); b) encapsulating ligands allow tuning of the core accessibility to oxygen to optimize probe's sensitivity in the physiological pO₂ range; and c) outer layer provides solubility and isolates the probe from interactions with endogenous biological species (proteins, nucleic acids, membranes etc) in order to maintain the calibration constants for quantitative pO₂ measurements in biological environments.

Both aforementioned patents teach compounds based on complexes of metals, such as Pd and Pt, with porphyrins and aromatically π-extended porphyrins, such as, for example, tetrabenzoporphyrin, tetranaphthaloporphyrin, tetraanthraporphrin and various derivatives thereof, which play the role of phosphorescent cores (part 1). These complexes possess bright room temperature phosphorescence, and Pd and Pt complexes of tetrabenzoporphyrins and tetranaphthaloporphyrins are especially desirable because they show strong light absorption in the near IR region (610-650 nm and 700-720 nm, respectively), where tissue is practically transparent. Moreover, Pd tetrabenzoporphyrins (PdTBP) and their derivatives have been shown to have long-lived phosphorescence (˜250 μsec) with quantum yields of 0.08-0.10%. These values have been later re-measured against improved fluorescence standards used throughout the remainder of this specification, and shown to be 0.0015-0.04 (see Esipova et al, Anal. Chem. 83:8756 (published on-line Oct. 11, 2011).

Generally, the surrounding environment determines properties of the phosphorescent probe with respect to oxygen measurement, including water solubility, toxicity, oxygen quenching constant, sensitivity of the measurements to chemically active components of tissue, and ease of excretion of the probe from the body through the kidney. It is also desirable to design the surrounding environment, such that it comprises an inert globular structure around the phosphor, through which only small uncharged molecules, i.e., oxygen, can diffuse into the close vicinity of the phosphorescent core for efficient quenching.

The '865 patent above teaches that the optimal surrounding environment for the phosphorescent core is made of dendrons as encapsulating ligands (part 2) and polyethyleneglycols (or oligoethyleneglycols) as the outer layer of the probe (part 3). (Note that together the encapsulating dendrons are said to comprise a dendrimer. Accordingly, the corresponding phosphorescent probes are termed dendritic.) Dendritic probes so far have shown to be superior phosphors for oxygen measurements in biological systems. Many laboratories around the world currently use these molecules for oxygen measurements in the blood, tissue interstitial space, various organs and with application of different modes of the phosphorescence quenching method (see above). See, e.g., Sakadzic et al., Nat. Methods 7:755 (2010); Devor et al., J. Neuroscience 31:13676 (2011); Lecoq et al., Nature Medicine 17:893 (2011); and since the effective filing date of this application, Parpaleix et al., Nature Medicine 19:241-246 (2013), which have capitalized on the use of the dendritic oxygen probes to decipher brain energy metabolism in the field of neuroscience. Thus the prior and present art have clearly established tremendous value of dendritic oxygen probes, warranting their further improvement and optimization.

It has therefore been an ongoing need in the art to further improve on the structure of dendritic phosphorescent probes by altering and improving their chemical structure, thereby providing a “next generation” of oxygen sensors with substantially improved phosphorescence emission for better imaging capabilities, ease of use, and range of applicability. In addition, some of the new molecules in this disclosure provide measurements of oxygen, not only in an aqueous environment, but also in liquid organic media, such as organic solvents and/or oils.

SUMMARY OF THE INVENTION

It is an object of the present invention to provide phosphors comprising a new class of porphyrin-based oxyphors and schemes for synthesizing the same, wherein the porphyrin is made less flexible and more planar, two modifications that the inventors have shown significantly (5-10 fold) increases the quantum yield over the prior art probes, and therefore serve as the bases for significantly improved oxygen sensors. These structurally improved, extended porphyrins are then complexed with dendrimers to surround the phosphorescent core by supramolecular structures which are designed to be highly soluble in either water based media or in liquid organic media, such as organic solvents and/or oils. They provide additional sought-after characteristics of phosphorescent probes such as long-lived phosphorescence and high quantum yields.

Additional objects, advantages and novel features of the invention will be set forth in part in the description, examples and figures which follow, all of which are intended to be for illustrative purposes only, and not intended in any way to limit the invention, and in part will become apparent to those skilled in the art on examination of the following, or may be learned by practice of the invention.

BRIEF DESCRIPTION OF THE DRAWINGS

The foregoing summary, as well as the following detailed description of the invention, will be better understood when read in conjunction with the appended drawings. It should be understood, however, that the invention is not limited to the precise arrangements and instrumentalities shown.

FIG. 1 illustrates an exemplary synthesis of meso-unsubstituted TBP, wherein M is an element selected from H₂, Zn, Ni, CU, Pd, Pt, Ru, Au, Os, Ir, La. Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu.

FIG. 2 depicts DAPIP and TAPIP porphyrins resulting from the disclosed synthesis scheme, with element M being selected from H₂, Zn, Ni, CU, Pd, Pt, Ru, Au, Os, Ir, La. Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu.

FIG. 3 depicts the synthesis of meso-unsubstituted TAPIP.

FIG. 4 depicts the synthesis of meso-unsubstituted DAPIP.

FIGS. 5A-H depict the absorption and emission spectra of selected metal complexes of TAPIP and DAPIP in dimethylformamide at 22 degrees Celsius; FIG. 5A shows the absorption spectra of ZnTAPIP; FIG. 5B shows the fluorescence of ZnTAPIP; FIG. 5C shows the absorption spectra of PdTAPIP; FIG. 5D shows the phosphorescence of PdTAPIP; FIG. 5E shows the absorption spectra of PtTAPIP; FIG. 5F shows the phosphorescence of PtTAPIP; FIG. 5G shows the absorption of PtDAPIP: FIG. 5H shows the phosphorescence of PtDAPIP.

FIG. 6 depicts the 2PA spectra of PtTAPIP as a solid line and the 2PA spectra of PdTAPIP as a dashed line, both in dimethylacetamide at 22 degrees Celsius.

FIG. 7 illustrates exemplary dendrimerization of porphyrins: i) peptide coupling; ii) hydrolysis.

FIG. 8 illustrates an exemplary dendritic phosphorescent probe modified with hydrophobic residues to allow oxygen measurements in liquid organic solutions, e.g., saturated alkanes, mineral oils etc., wherein M is an element selected from H₂, Zn, Ni, CU, Pd, Pt, Ru, Au, Os, Ir, La. Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu.

DETAILED DESCRIPTION OF CERTAIN EMBODIMENTS OF THE INVENTION

The present invention provides highly efficient and highly soluble phosphorescent probes suitable for measurements of oxygen in tissue of animals and humans. Inventive probes are surrounded by an inert globular structure, an example of which is derivatized PdTBP (Pd tetrabenzoporphyrins) surrounded by three-dimensional supramolecular structure known as a “dendrimer,” which is well understood in the field.

Oxygen levels in biological systems can thus be measured by the phosphorescence quenching method using probes with controllable quenching parameters and defined biodistributions. A general approach is provided to the construction of phosphorescent nanosensors with tunable spectral characteristics, variable degrees of quenching, and a high selectivity for oxygen that are soluble in aqueous or organic solvents (e.g., benzene, toluene, hexane, octane, tetrahydrofurane, mineral oil, and the like), permitting phosphorescence measurements throughout the entire ambient oxygen range: pO₂=0-160 mm Hg. The probes are based on bright phosphorescent Pt and Pd complexes of porphyrins and symmetrically π-extended porphyrins (tetrabenzoporphyrins and tetranaphthoporphyrins).

In certain embodiments of the invention, π-extension of the core macrocycle provides tuning of the spectral parameters of the probes in order to meet the requirements of a particular imaging application (e.g., oxygen tomography versus planar microscopic imaging). Metalloporphyrins are encapsulated into poly(arylglycine) dendrimers, which fold in aqueous environments and create diffusion barriers for oxygen, making it possible to regulate the sensitivity and the dynamic range of the method. The periphery of the dendrimers is modified with poly(ethylene glycol) residues, which enhance the probe's solubility, diminish toxicity, and help prevent interactions of the probes with the biological environment. The probe's parameters were measured under physiological conditions, and the probes were shown to be unaffected by the presence of biomacromolecules.

The performance of the probes was demonstrated in applications, including in vivo microscopy of vascular pO₂ in the rat brain.

As used herein, “DAPIP” shall mean a meso-unsubstituted diphthalimidoporphyrin.

As used herein, “TAPIP” shall mean a meso-unsubstituted tetraphthalimidoporphyrin.

As used herein, 1P shall mean “one-photon.”

As used herein, 2P shall mean “two-photon.”

As used herein, 2PA shall mean “two-photon absorption.”

As used herein, 2PLM shall mean “two-photon phosphorescence lifetime microscopy”.

I. Principles of Phosphorescence Quenching Method and Requirements of In Vivo Oxygen Probes

Phosphorescence quenching relies on the ability of molecular oxygen, which is a triplet molecule in the ground state (O₂X³Σ_(g) ⁻), to react with molecules in their excited states, quenching their luminescence. Collisional quenching is much less probable on the time scale of singlet excited states (nanoseconds) than of triplet states (microseconds to milliseconds), making phosphorescence significantly more sensitive to oxygen than fluorescence. Assuming a large excess of oxygen relative to the concentration of triplet emitters—a condition typically met in biological environments—the dependence of the phosphorescence intensity and lifetime on oxygen concentration follows the Stern-Volmer relationship: I₀/I=τ₀/τ=1+K_(SV)[O₂],  [Equation 1]

where I and τ are the phosphorescence intensity and the lifetime at oxygen concentration [O₂] and in the absence of oxygen (I₀, τ₀); and K_(SV) is the Stern-Volmer quenching constant.

In practice, using lifetime τ as the analytical signal for [O₂] is more accurate, because the lifetime is independent of the probe distribution and of any other chromophores present in the biological system. where τ is the phosphorescence lifetime at oxygen concentration at a specific oxygen pressure [pO₂]; τ₀ is the phosphorescence lifetime in the absence of oxygen [pO₂=0]; and k_(q) is the Stern-Volmer quenching constant. See, Lebedev et al., ACS Appl. Mater. Interfaces 1:1292 (2009); Finikova et al., Chem Phys Chem 9:1673 (2008); Sakad et al., Nat. Methods 7:755 (2010); Lecoq et al., Nat. Med. 17:893 (2011); Vinogradov & Wilson, In Designing Dendrimers, Campagna, Ceroni, Puntoriero, Eds.; Wiley: 2012.

Among the attractive features of the phosphorescence quenching technique are its high specificity, submillisecond temporal response, high sensitivity, and relative simplicity of instrumentation. When soluble probes are used, calibration of the method is absolute in a sense that the probes' quenching parameters must be determined only once, and then they may be used thereafter for measurements under similar conditions.

It is customary to express oxygen content in the units of pressure (mm Hg) rather than concentration (M), since in the majority of biological experiments partial pressure of oxygen (pO₂) is the actually controlled experimental parameter. At 298 K and the air pressure of 760 mm Hg (oxygen fraction in the air is 21% or 159.6 mm Hg), air-equilibrated aqueous solutions are 252 μM in O₂ (Fogg, et al., “Solubility of gases in liquids. Wiley, New York, 2001). However, for simplicity the pressure of water vapor above the solution is neglected, although at higher temperatures it will rise and, consequently, the partial pressure of oxygen (pO₂) will decrease. This assumes that the Henry's law holds in the physiological range of oxygen concentration: [O₂]=α×pO₂, where α is the oxygen solubility coefficient (M×mm Hg⁻¹) for the bulk phase. Considering K_(SV)=k₂τ₀, where k₂ is the bimolecular rate constant for the quenching reaction, Equation 1 can be rewritten as: 1/τ=1/τ₀+(k _(q))(pO₂]  [Equation 2]

where k_(q)=αk₂ and has the units of mm Hg⁻¹s⁻¹. Equation 2 contains two parameters specific to the molecule of the probe: constant k_(q) and lifetime τ₀. Their interplay defines the sensitivity and the dynamic range of the method. For analytical purposes, it is desirable that the measurement parameter, which is the phosphorescence lifetime τ herein, spans the largest possible interval of values throughout the range of analyte concentrations, assuring highest possible measurement resolution. To quantify the dynamic range of lifetimes, parameter R=(τ₀−τ_(air))/τ₀ is used, wherein τ₀ (pO₂=0 mm Hg) and τ_(air) (pO₂=159.6 mm Hg) are the maximal and the minimal values of the phosphorescence lifetimes in physiological experiments. Another important parameter is the signal-to-noise ratio (SNR), which is obviously higher for probes with larger emission quantum yields (assuming the same emission wavelengths).

Pt and Pd porphyrins are typically used as phosphorescent chromophores for oxygen measurements in biological systems (vide infra). Triplet lifetimes of Pd porphyrins in deoxygenated solutions at ambient temperatures are in the range of hundreds of microseconds (abbreviations have their normal meaning herein, but microseconds are specifically referred to “μs” or “μsec” herein), and their phosphorescence quantum yields in the absence of oxygen (ϕ₀ are typically 0.05-0.1. (Eastwood et al., J. Molecular Spectroscopy 35:359 (1970)). For Pt porphyrins the corresponding values are tens of microseconds and 0.10-0.25 (Id.; Kim et al., J. Amer. Chem. Soc. 106:4015 (1984)), respectively. Constants k_(q) for “unprotected” metalloporphyrins in aqueous solutions are ˜3,000 mm Hg⁻¹s⁻¹. To illustrate how quenching constants k_(q) and lifetimes τ₀ affect oxygen measurements, consider two probes, PdP and PtP, representing some arbitrary Pd and Pt porphyrins: τ₀ (PdP)=500 μs, τ_(o)(PtP)=50 μs; ϕ₀ (PdP)=0.05, ϕ₀ (PtP)=0.10, where subscript “0” indicates pO₂=0 mm Hg.

When the quenching constant is high, e.g., k_(q)=3,000 mm Hg⁻¹s⁻¹, the lifetime of PdP decreases from τ₀=500 μs to τ_(air)=2.1 μs, resulting in a large dynamic range (R≈0.996). However, between about 20 mm Hg and air saturation, the lifetime changes by no more than 3% of the total value, between 16 μs and 2.1 μs. Moreover, already at 10 mm Hg. the probe's quantum yield becomes extremely low (ϕ<0.003) due to the excessive quenching. Consequently, a probe like PdP is useful only in a very low range of oxygen concentrations, probably not higher than at pO₂˜5 mm Hg.

Due to its higher quantum yield and shorter τ₀, probe PtP can be used up to about 50 mm Hg (τ=5.9 μs), but above that limit its lifetime also changes very weakly, by no more than ˜3 μs. The lifetime dynamic range of PtP (R≈0.96) is not very different from that of PdP; but if the quenching constant were to be reduced or decrease, which is inevitable upon binding of the probe to proteins in vivo (vide infra), this probe would become insensitive to changes in oxygenation.

For higher sensitivity, probes with a greater τ₀ are preferred, but only if their phosphorescence changes gradually instead of being highly quenched already at very low oxygen concentrations. Such adjustment of sensitivity can be achieved by varying constants k_(q). Overall, it is clear that control over the values of the quenching constants and the ability to keep them unaltered in measurement environments is the key to accurate oxygen measurements. All comparative terms, e.g., higher, lower, increased, decreased, enhanced, reduced, faster, slower, etc, assume their accepted standard dictionary meanings herein, preferable as compared to a stated molecule, probe, compound, or the like.

Phosphorescence quenching by oxygen typically occurs much faster than the diffusion of the reactants and formation of encounter complexes; and in the majority of cases, diffusion can be considered the rate-limiting step for oxygen quenching reaction. (Turro, Modern Molecular Photochemistry, University Science Books, Sausalito, C A, 1991). By altering oxygen diffusion coefficients in the local vicinity of the phosphorescent chromophores, constants k_(q) can be regulated. Such tuning can be achieved by means of dendritic encapsulation.

Additional requirements for phosphorescent probes for medical imaging of oxygen include lack of toxicity and preferably excretability from the blood upon completion of imaging. Globular uncharged molecules with molecular weights up to about 15 kDa are usually excretable by the kidney (Caliceti et al., Advanced Drug Delivery Reviews 55:1261-1277 (2003). If a probe satisfies this criterion and remains confined to the intravascular space (does not diffuse out of the blood vessels), it is likely to be removed from the blood by the kidney-mediated dialysis, and the possibility of long-term toxicity effects can be avoided. Of course, for animal studies, excretability is not as stringent a requirement, whereas confinement to a particular tissue compartment (intravascular, interstitial or intracellular) can be very important. In that case, probes of larger sizes may become advantageous.

This leads to a molecular design comprising a bright phosphorescent chromophore with sufficiently long triplet lifetime τ₀ and a protective jacket, whose purpose is to constrain oxygen diffusion in the local environment of the chromophore. The dendrimer itself must be hydrophobic to permit it to fold (or collapse) in polar solvents, such as water, around the porphyrin. Otherwise, if it were hydrophilic, it would spread branches freely and create no effective barrier for oxygen diffusion to the porphyrin. Importantly, “hydrophobic” does not necessarily mean lipophilic. In other words, a compound that “does not like water” (like the arylglycine (AG) dendrimers defined below) does not mean that it always “likes” every possible type of organic media. For example, the inventors' arylglycine dendrimers fold both in water and in many organic solvents, such as, but not limited to tetrahydrofuran (THF), oils, hexanes, and the like. However, in other organic solvents, such as dimethylformamide (DMF) or dimethylsulfoxide (DMSO), they would spread branches and would not fold. As a result, such dendrimers would not provide a barrier for oxygen in DMF and DMSO; but they would do so in water, THF, oils, alkanes etc.

The periphery of the probe must be hydrophilic and inert in order to prevent interactions with components of the biological system (e.g., bio-macromolecules, cellular membranes). The overall size of the molecule should be large enough to prevent probe leakage through the vascular walls, but yet small enough to allow removal through the kidney, if excretability is desired. Alternatively, the periphery of the probe must be hydrophopbic if the measurement is to be conducted in oils, alkanes, etc.

A novelty of the present invention lies in making the folded molecules soluble. That is accomplished by adding an outer layer to the dendrimer, and it is the outer layer that then takes the probe into solution, even when the dendrimer itself is folded and poorly soluble. Consequently in the present invention, to dissolve a folded dendrimer in water, a hydrophilic outer layer of polyethyleneglycols (PEG) is added to permit dissolution; but when e.g., oils or long alkyl chains are added to the outer layer, the dendrimer is then soluble in liquid organic compounds.

Overall the problem of keeping the diffusional accessibility of the phosphorescent chromophore to oxygen in biological environments constant throughout the studied object and the calibration unchanging, is by far the biggest challenge in the design of phosphorescent oxygen probes. Moreover, this problem is inherent in all methods relying on kinetics of oxygen diffusion. To overcome this difficulty, design of a molecular oxygen sensor entails construction of a well-defined microenvironment around the phosphorescent chromophore in order to isolate it from interactions with other molecules, except for oxygen. Dendritic encapsulation (Hecht & Fréchet, Angewandte Chemie-International Edition 40:74 (2001); Gorman & Smith, J. Amer. Chem. Soc. 122:9342 (2000)) arguably provides one of the most straightforward ways to construct monodisperse, well-defined molecular jackets around luminescent chromophores (Balzani et al., Functional and Hyperbranched Building Blocks, Photophysical Properties, Applications in Materials and Life Sciences 228:159 (2003); Ceroni et al., Progress in Polymer Science 30:453 (2005)).

II. Phosphorescent Cores of Dendritic Oxygen Probes

The key photophysical properties required for biological oxygen sensing are strong absorption, preferably in the near infra-red region (NIR) of the spectrum (near infrared region of tissue is approximately 600 nm to 1000 nm, but for excitation purposes from ˜600 or ˜620 to ˜900 or ˜1000 nm is appropriate) to minimize the interference by the natural tissue chromophores (e.g., heme containing proteins, carotenoids), and strong long-lived phosphorescence in solutions at ambient temperatures. Very few chromophores possess such properties. Among them, metalloporphyrins emit from (π-π*) states, and exhibit significantly longer triplet lifetimes (Eastwood et al., J. Mol. Spectroscopy 35:359 (1970)), thus possessing much higher intrinsic sensitivity to oxygen.

Regular meso-tetraarylated Pt and Pd porphyrins with various peripheral substituents can be readily synthesized via, e.g., the Lindsey (Lindsey et al, J. Organic Chem. 52:827 (1987)) or Senge (Senge, Accounts of Chemical Research 38:733 (2005)) methods. Thermodynamic stabilities of these complexes are extremely high, (Buchler, Ch. 5 in Porphyrins and Metalloporphyrins, Smith, K. M. Ed., Elsevier, 1975, New York) entirely precluding release of free metal ions into biological environments and associated toxicity. The major drawback of using regular Pt and Pd porphyrins for in vivo applications is that their absorption bands, the so-called Q-bands, are positioned in the visible range (λ_(Q)˜520-530 nm; ε˜20,000 M⁻¹ cm⁻¹), thus overlapping with absorption of naturally occurring chromophores. Still, absorption in the visible region may be useful in planar wide-field phosphorescence imaging, where less diffuse nature of excitation serves to improve spatial resolution. In addition, absorption near 500 nm overlaps with emission of many two-photon (2P) chromophores, which is useful in construction of FRET-enhanced probes for two-photon oxygen microscopy (vide infra) (Finikova et al., Chem Phys Chem 9:1673 (2008)).

Many porphyrinoids possess near infrared absorption bands; however, very few have characteristics appropriate for oxygen sensing (Vinogradov & Wilson, J. Chem. Soc., Perkin Trans. II 103 (1995)). The most useful today are derivatives of so-called laterally π-extended (or π-expanded) porphyrins. Lateral π-extension of Pt and Pd porphyrins by annealing their pyrrole residues with external aromatic rings results in chromophores with dramatically red-shifted absorption bands and strong room-temperature phosphorescence (Ibid; Tsvirko et al., Optika i Spektroskopiya (Russ) 34:1094 (1973); Rozhkov et al., Inorganic Chemistry 42:4253 (2003)). Spectra of Pt analogs are very similar in shape, but are blue-shifted by ˜10-15 nm as compared to those of Pd counterparts.

An important feature of all porphyrin-based probes is their very large separation between the absorption and phosphorescence, achievable via excitation at the Soret bands (e.g., 9329 cm⁻¹ for Pd porphyrins). Efficient S₂→S₁ internal conversion, (Tripathy et al., J. Phys. Chem. A 112:5824 (2008)) combined with extremely high extinction coefficients of S₀-S₂ transitions (˜3×10⁵ M⁻¹ cm⁻¹) makes this pathway superior to the direct S₀-S₁ excitation in those cases when near UV radiation can be sustained by the biological object.

Until recently, synthesis of π-extended porphyrins presented a challenging problem. All synthetic methods were based on high temperature condensations between phthalimide (or naphthalimide) and arylacetic acids, or similar donors of benzo- and phenyl-groups (Kopranenkov et al., J. Gen. Chem. (Russ) 51:2165 (1981); Edwards et al., J. Amer. Chem. Soc. 98:7638 (1976); Ichimura et al., Inorganica Chimica Acta 176:31 (1990)). The harsh conditions of condensation (melting at 300-400° C.) allowed for only a few inert substituents, such as alkyl groups or halogens (Kopranenkov et al., Khimiya Geterotsiklicheskikh Soedinenii 773 (1988)) to be introduced into the porphyrin macrocycle. In addition, low yields and complex, inseparable mixtures of products made this approach impractical.

The newly emerged approaches to π-extended porphyrins rely on the Barton-Zard methodology (Barton et al., Tetrahedron 46:7587 (1990)) for synthesis of porphyrinogenic pyrroles, which give rise to precursor porphyrins requiring final aromatization. Two methods have been developed into practical synthetic schemes: one making use of retro-Diels-Alder reaction (Ito et al., Chemical Communications 1661 (1998); Ito et al., Chem. Comm. 893 (2000)), another relying on simple and efficient oxidative aromatization strategy (Finikova et al., Chem. Commun. 261 (2001); Finikova et al., J. Organ. Chem. 69:522 (2004)). The latter method is being used today to synthesize tetrabenzo- and tetranapthoporphyrins for construction of phosphorescent oxygen probes, as well as in several other applications.

Although meso-tetraarylated π-extended porphyrins are most common, primarily because of the solubility considerations, meso-unsubstituted tetrabenzoporphyrins (TBP's) and tetranaphthoporphyrins (TNP's), which in fact have higher phosphorescence quantum yields and longer lifetimes, can also be synthesized via the oxidative aromatization method (Finikova et al., J. Org. Chem. 70:9562 (2005)). Furthermore, recent introduction of 4,7-dihydroisoindole (Filatov et al., Europ. J. Org. Chem. 3468 (2007)) paved a practical route to 5,15-diaryl-TBPs (Filatov, et al., J. Org. Chem. 73:4175 (2008)). The latter porphyrins are especially attractive for construction of oxygen probes, as they combine higher emissivity (Lebedev et al., J. Phys. Chem. A 112:7723 (2008)) with the possibility of attaching dendrons to the anchor points in the meso-aryl rings, which is lacking in meso-unsubstituted porphyrins. Notably, examples of porphyrin-dendrimers based on 5,15-diarylporphyrins are well known (Dandliker et al., Angewandte Chemie-International (Edition in English) 33:1739 (1994); Dandliker et al., Angewandte Chemie-International (Edition in English) 34:2725 (1996)).

III. Polyglutamic Pd Porphyrin-Dendrimers

Polyglutamic Pd porphyrin-dendrimers made up the first generation of dendritic oxygen probes (Vanderkooi et al., J. Biol. Chem. 262:5476 (1987); Vinogradov & Wilson J. Chem. Soc., Perkin Trans. 2:103 (1995); Papkovsky et al., J. Fluoresc. 15:569 (2005)). The compounds are described by the general formula, e.g., PdP-(Glu^(n)OH)₁, if first generation, where n=1-4 (dendrimer generation) and Glu^(n)OH is the glutamic layer. Similar abbreviations to designate porphyrin dendrimers of different types and generations, terminated by different groups are used herein. But the polyglutamic Pd porphyrin-dendrimers required prebinding to macromolecular carriers (e.g., albumin) in order to enhance their aqueous solubility and bring their quenching parameters (τ₀ and k_(q), Eq 1) into the range compatible with physiological oxygen concentrations (see Vinogradov & Wilson, In Designing Dendrimers, chap 14, Campagna, Ceroni, Puntoriero, Eds.; Wiley: 2012) for discussion). However, foreign albumin was a potential source of toxicity and immunogenic responses.

Introduction of polyglutamic dendritic porphyrins Vinogradov et al., Chem. Eur. J. 5:1338 (1999); Vinogradov et al., Adv. Exp. Med. Biol. 428:657 (1997); Rietveld et al., Tetrahedron 59:3821 (2003), which were generation 2 (gen 2) polyglutamic PD prophyrin dendrimers, known as Oxyphors R2 and G2 (Dunphy et al., Anal. Biochem. 310:191 (2002)), offered a partial solution to this problem, and they have been used in many biological studies over the years, wherein dendritic encapsulation was needed to protect the triplet states of Pd porphyrins from oxygen quenching. Polyglutamic probes have high intrinsic aqueous solubility and can be introduced into the blood directly without prebinding to albumin. When in the blood, they form complexes with endogenous albumin, and these complexes serve as ultimate oxygen sensors. But as a result, use of Oxyphors R2 and G2 is limited to albumin-rich environments, such as blood plasma (>2% in albumin by weight). But even in such environments, incomplete binding to albumin, which can be easily encountered at higher probe concentrations (e.g., above ˜10⁻⁵ M), may lead to heterogeneity of the probe signal, skewing the measurement. (Vinogradov et al., Applied Spectroscopy 54:849 (2000)). Notably, combinations of polyglutamic probes with polymeric nanoparticle-based carriers have been recently introduced (e.g., Lee et al., Anal. Chem. 82:8446 (2010)) which alleviate the necessity of albumin binding and allow oxygen measurements in cultured cells.

Thus, the drawbacks associated with use of dendritic polyglutamic porphyrins clearly show that probes with albumin-independent phosphorescence lifetimes and oxygen quenching constants would greatly simplify data analysis and broaden applicability of the method (e.g., make it possible to take measurements in albumin-free environments). Although polyglutamic dendrimers were limited in use, experiments showed that composition of the dendritic matrix is at least as important for shielding as is the dendrimer size itself, leading to studies of the interplay between the dendrimer composition, size and encapsulating efficiency, as measured by oxygen diffusion and quenching of phosphorescence.

IV. Influence of Size and Composition of Dendritic Matrix on Oxygen Shielding Efficiency

In order to determine which dendrimers provide optimal attenuation of oxygen quenching of porphyrin phosphorescence a study was performed (Rozhkov et al., Macromolecules 35:1991 (2002)) which involved three types of porphyrin-dendrimers: Fréchet-type poly(aryl ethers) (Hawker et al., J. Chem. Soc. Perkin Trans. I 1287 (1993)), Newkome-type poly(ether amides) (Newkome et al., Macromolecules 24:1443 (1991); Newkome et al., Synlett 53 (1992)), and polyglutamates (Vinogradov et al., Chemistry-A European J. 5:1338 (1999)).

Pd-meta-octahydroxyphenylporphyrin and Pd-meta-octacarboxyphenyl-porphyrin, compatible with either Williamson (Fr) or peptide (Nw, Glu) chemistries, were used as phosphorescent cores. The studies were performed in dimethylformamide (DMF), tetrahydrofuran (THF) and water. To insure appropriate aqueous solubility, termini of the dendrimers were modified with oligoethyleneglycol residues, e.g., PEG (polyethylene glycol) which rendered uncharged molecules soluble both in organic solvents and in water.

In organic solvents, decrease in the quenching rates was found to be consistent with increase in the dendrimer size, and these changes were rather insignificant. As expected, bulkier poly(ether amides) exhibit a stronger effect, but still the decrease in the quenching was only about 75% for G2 dendrimer, whose weight is more than 12 kDa, that is more than 12 times that of the core porphyrin. Notably, in the case of polyglutamic derivatives of PdTCPP, dendrons were attached to the para-positions on the meso-aryl rings of the porphyrin, extending out of the macrocycle instead of covering it from above and below, and thus the shield effect was much weaker for the same size dendrons. A much larger difference in quenching rates was observed in water.

The practical determination was that dendrimers constructed from aromatic building blocks potentially have much higher shielding efficiency in aqueous environments than do other types of dendrimers. In addition, it was determined that in order to prevent interaction of dendrimers with biological macromolecules, their periphery should be modified with PEG residues (vide infra), referred to as “peripheral PEGylation” of the dendrimers.

Other references relating to dendritic macromolocules and their methods of production can be found in U.S. Pat. Nos. 5,418,301; 4,568,737; 5,393,795; 5,256,193; 5,393,797; 5,393,795; 5,393,797; 5,098,475; 5,041,516 and 4,568,737, the entire disclosures of which are incorporated herein by reference. The phosphors employed in, for example, U.S. Pat. No. 5,837,865 (the '865 patent), and by Vinogradov and Wilson, J. Chem. Soc., Perkin trans. 2:103-111 (1995), were preferably of the general formula described therein, wherein R₁ was hydrogen (H) or substituted or unsubstituted aryl. R₂ and R₃ were independently hydrogen or are linked together to form substituted or unsubstituted aryl. When R₂ and R₃ were linked together to form an aryl system, the aryl system was necessarily in a fused relationship to the respective pyrrole substrate. M was H₂ or preferably a metal selected from the group consisting of Lu, Pd, Pt, Zn, Al, Sn, Y La, and derivatives thereof, with Pd, Pt and Lu being most preferred.

Accordingly, the prior art formulations were all based on meso-tetraaryl-substituted metalloporphyrins, but the inventors have determined that non-planar deformation of the porphyrin macrocycle resulting from tetra-aryl substitution led to a loss of phosphorescence emission. Thus, the resulting dendritic oxygen probes were effective, but limited for their intended purpose.

V. Protected Dendritic Probes: Oxyphors G4 and R4

Subsequently however, the inventors identified a general approach to protected molecular oxygen probes, which do not require albumin or any other supporting macromolecular carriers or nanocompositions (See, Lebedev et al., ACS Appl. Mater. Interfaces 1:1292 (2009); Finikova et al. Chem Phys Chem 9:1673 (2008); Ceroni, et al., Photochem. Photobiol. Sci. 10:1056 (2011)). In these probes, phosphorescent metalloporphyrins are encapsulated inside hydrophobic dendrimers, which form protecting shells, enveloping the chromophores, controlling oxygen diffusion to the excited triplet states, and enabling control over the sensitivity of the approach. Peripheral PEGylation of the dendrimers ensured high aqueous solubility and prevented interactions of the probes with biological macromolecules.

Synthesis and detailed characterization of two new probes, Oxyphors R4 and G4, derived from phosphorescent Pd-meso-tetra-(3,5-dicarboxyphenyl)-porphyrin (PdP) or Pd-meso-tetra-(3,5-dicarboxyphenyl)-tetrabenzoporphyrin (PdTBP), respectively, as reported by Esipova et al, Anal. Chem. 83:8756 (published on-line Oct. 11, 2011), herein incorporated by reference. These probes are built according to the above-referenced general scheme, and possess features common for protected dendritic probes, i.e., hydrophobic dendritic encapsulation of phosphorescent metalloporphyrins and hydrophilic PEGylated periphery. The new Oxyphors R4 and G4 are highly soluble in aqueous environments and do not permeate biological membranes. The probes were calibrated under physiological conditions (pH 6.4-7.8) and temperatures (22-38° C.), showing high stability, reproducibility of signals, and lack of interactions with biological solutes were intended for wide use in biological research. However, the probes' structural elements are further optimized for improved yield of synthesis, 1-2 times higher monodispersity of pure monodisperse dendritic oxygen probes, lack of aggregation in aqueous solutions, and overall better chemical stability.

As disclosed above a byproduct of the biological oxygen measurements by phosphorescence quenching using exogenous phosphorescent probes introduced directly into the medium of interest (e.g., blood or interstitial fluid) is singlet, a highly reactive species capable of damaging biological tissue. Consequently, because potential probe phototoxicity is a concern for biological applications studies compared the ability of polyethyleneglycol (PEG)-coated Pd tetrabenzoporphyrin (PdTBP)-based dendritic nanoprobes of three successive generations to sensitize singlet oxygen. As a result, it was demonstrated that the size of the dendrimer has practically no effect on the singlet oxygen sensitization efficiency in spite of the strong attenuation of the triplet quenching rate with an increase in the dendrimer generation.

Nevertheless, in spite of their ability to sensitize singlet oxygen, the phosphorescent probes were found to be non-phototoxic when compared with the commonly used photodynamic drug Photofrin in a standard cell-survival assay. (Ceroni et al., Photochem. Photobiol. Sci. 10:1056-1065 (2011)). The lack of phototoxicity is presumably due to the inability of PEGylated probes to associate with cell surfaces and/or penetrate cellular membranes. In contrast, conventional photosensitizers bind to cell components and act by generating singlet oxygen inside or in the immediate vicinity of cellular organelles. Therefore, PEGylated dendritic probes are safe to use for tissue oxygen measurements as long as the light doses are less than or equal to those commonly employed in photodynamic therapy.

One of the probes, Oxyphor G4 was applied to imaging of oxygen distributions in tumors, both intravascularly and in the interstitial space. The probe allowed dynamic visualization of the tissue pO₂ levels in the tumor and in the surrounding muscle, as oxygenation responded to changes in the depth of anesthesia. The phosphorescence from the probe also could be detected in trans-illumination geometry, i.e., through the whole body of the animal, thus demonstrating feasibility of in vivo full body oxygen tomography.

VI. Effect of the Dendrimer Outer Layer

Although it is critically important that quenching properties of phosphorescent probes do not change in the presence of blood plasma proteins and other biological macromolecules, quenching constants of all carboxylate-terminated porphyrin-dendrimers were found to be highly sensitive to albumin. For example, k_(q) of gen 2 Fréchet-type porphyrin dendrimer in albumin solution (2% by mass) is five times lower (30 mm Hg⁻¹ s⁻¹) than that in the albumin-free aqueous buffer (151 mm Hg⁻¹ s⁻¹) (Gorman et al., J. Amer. Chem. Soc. 122:9342 (2000)). To the contrary, however, quenching of porphyrin-dendrimers modified with oligoethyleneglycol residues (PEG350, Av. MW=350) appeared to be unaffected by serum proteins. Thus, k_(q) of the PEGylated analogue of gen 2 Fréchet-type porphyrin dendrimer was found to have the same value (130 mm Hg⁻¹s⁻¹) in the presence and in the absence of albumin (Estrada et al., Optics Letters 33:1038 (2008)).

Thus, it was important to distinguish between the effect of hydrophobic dendrons and the effect of external PEG residues. While the latter also contribute to the protection from quenching, especially at early dendritic generations, the net effect of PEG is very small, as noted above, compared to the shielding by dendritic branches. Moreover, the PEG effect rapidly levels off with extension of linear chains. It was shown that external PEG chains as large as 300,000 Da have practically no effect on oxygen quenching constants of these molecules. Moreover, in addition to being able to prevent interactions of dendrimers with proteins, peripheral PEG groups also strongly affect biodistribution and rate of excretion of dendritic macromolecules (Newkome, supra, 1992).

VII. Aryl-Glycine Dendrimers and Fully Protected Phosphorescent Probes

Among known dendrimers with aromatic backbones, dendritic arylamides were very attractive because of their high chemical stability, low cost and effective protocols available for their assembly. In particular, arylamide dendrimers based on 5-aminoisophthalic acid (5-AIPA) were selected to make the focal functionality more reactive and to simultaneously increase the flexibility of the dendritic backbone by extending the amino-end of the 5-AIPA molecule by adding a flexible fragment, terminated with an aliphatic amine. This possibility was explored by constructing aryl-glycine (AG) dendrons and dendrimers (Vinogradov, Organic Letters 7:1761 (2005)). The following abbreviations are used to designate aryl-glycine dendrons and dendrimers. Dendrons were designated X-AGnR, where AG denotes the dendritic aryl-glycine skeleton, n is the dendrimer generation number, X is the focal functionality and R is the terminal group. Dendrimers were designated C-(AGnR)m, where C denotes the dendrimer core, AG denotes the dendritic aryl-glycine skeleton, n is the generation number, R is the terminal group and m is the number of dendritic wedges attached to the core.

The developed synthesis of AG dendrons relies on the classic Fischer's haloacyl halide method (Miller et al., Chem. Mater. 2:346 (1990)) for the synthesis of building blocks. Synthesis of AG-dendrons in principle also can be implemented using the Fischer's method, however, a more robust scheme is based on a coupling-deprotection sequence employing the peptide-coupling reactions of Lebedev et al., ACS Applied Materials & Interfaces 1:1292 (2009)). See also synthesis and peptide-coupling reactions described in greater detail in Vinogradov & Wilson, In Designing Dendrimers, chap 14, Campagna, Ceroni, Puntoriero, Eds.; Wiley: 2012).

Each step of the sequence was carefully optimized in order to insure maximal yields and monodispersity of the probes. Porphyrins modified with AG¹ and AG² (aryl-glycine, first and second generation) dendrons could be isolated in high purity, but modification of porphyrins with AG³-dendrons (third generation) proved extremely challenging, always yielding mixtures of dendrimers with six, seven and eight dendritic branches. The peripheral ester groups were hydrolyzed using a special two-step procedure (Lebedev et al., supra, 2009), which in parallel destroys unreacted dendrons, making it possible to entirely avoid chromatographic purifications. The resulting peripheral carboxyl groups on the dendrimers are esterified with PEG residues of the desired length, and simple re-precipitation from THF upon addition of diethyl ether produced pure PEGylated dendrimers. The magnitude of the attenuation effect is similar to that of poly(aryl ether) dendrimers. As a result quenching constants and lifetimes of gen 2 Pd porphyrin-dendrimers are well suited for biological oxygen measurements. These probes exhibit good dynamic range and excellent sensitivity. For example, in the case of PdP-based gen 2 dendrimer the relative sensitivity coefficient R (vide supra) is as high as 0.9. Moreover, PEG-coated AG porphyrin-dendrimers exhibited a property that their oxygen quenching constants kq and lifetimes τ₀ are completely insensitive to the presence of biological macromolecules.

VIII. Improvements in the “Next Generation” of Oxygen Sensors: Meso-Unsubstituted Porphyrin Embodiments.

A) Increased Emission Output (Quantum Yield) of Phosphorescent Porphyrin-Based Probes.

Systematic structure/property comparisons between differently substituted porphyrins, have demonstrated that dendritic oxygen probes can be constructed using Pd meso-unsubstituted.

Increase in the phosphorescence quantum yield is an important objective. Pd meso-tetraarylporphyrins have their quantum yields at zero-oxygen in the range of 0.02-0.08 and triplet lifetimes of 300-700 μs, depending on the type of π-extension, i.e., tetrabenzo-extension or tetranaphtho-extension with respect to the basic 18-tetrapyrrolic macrocycle (Rozhkov et al., Inorg. Chem. 42:4253-4255 (2003); Rogers et al., J. Physical Chem. A 107:11331-11339 (2003)). Analogous Pt porphyrins have the quantum yields of 0.10-0.20, when measured by currently approved measurement techniques, and their lifetimes are 30-60 μs.

The inventors' detailed photophysical, structural and computational studies were conducted to delineate the interplay between radiative and non-radiative triplet deactivation processes in Pd porphyrins and tetrabenzoporphyrins (see Lebedev et al., J. Physical Chem. A, 112:7723-77336 (2008)). In fact, non-planar distortions of the porphyrin macrocycle were shown to diminish the triplet emission yield of PdTBP's competing non-radiative triplet-to-singlet ground state transitions, i.e., intersystem crossing. This is because the lifetime of the PdTBP triplet state in the absence of oxygen increases with dendritic generation, thus compensating for the concomitant decrease in the rate of quenching. In fact, non-planar distortions of the porphyrin macrocycle were shown to diminish the triplet emission yield of PdTBP's by increasing the rate of T₁→S₀, referring to the internal, non-radiative quenching of the triplet state (T₁) (returning it to the ground state (S₀). Increase in this non-radiative pathway decreases phosphorescence emission. However, this effect is considerably less pronounced than in regular non-extended porphyrins. Photophysical measurements show that non-planar deformations have deleterious effect on the porphyrin triplet emissivity. Therefore, even highly saddled tetraaryl-TBP's, which are used as cores in current probes, are able to phosphoresce.

It was also determined by the inventors' studies that Pd and Pt TBP's without meso-substituents (Finikova et al., J. Org. Chem. 70:9562-9572 (2005A)) have much higher emission quantum yields than the corresponding tetraarylporphyrins. In the case of meso-unsubstituted PtTBP's, phosphorescence quantum yields reach as high as 0.5 at room temperature, by currently accepted measuring techniques. The same trends are characteristic of TNP's.

Based on these findings, Pt and Pd meso-unsubstituted TBP's and TNP's are used for construction of certain embodiments of the new generation probes of the present invention.

In one embodiment of the present invention, the porphyrinogens are assembled using the 2+2 (Filatov et al., “Synthesis of 5,15-diaryltetrabenzoporphyrins,” J. Org. Chem. 73:4175. (2008)) and oxidized by DDQ (dichlorodicyano-1,4-benzoquinone) into the target precursor tetracyclo-hexenoporphyrin (TCHP) (Ibid). After insertion of Pd or P), the TCHP is oxidized, also by DDQ, into target TBP's (Finikova et al., “Novel versatile synthesis of substituted tetrabenzoporphyrins,” J. Org. Chem. 69:522 (2004)).

Synthesis of meso-unsubstituted TBP's and TNP's with substituents in the fused rings has been previously developed (Finikova et al., “Synthesis and luminescence of soluble meso-unsubstituted tetrabenzo- and tetranaphtho [2,3] porphyrins,” J. Org. Chem. 70:9562 (2005)). However, these positions are hindered sterically, especially with respect to the attachment of bulky dendritic ligands, required for “protection” of the porphyrin core from excessive oxygen quenching.

In an embodiment of the invention, the scheme depicted in FIG. 1 is used to synthesize meso-unsubstituted TBP's with appropriately positioned anchor groups as disclosed, with M being selected from H₂, Zn, Ni, CU, Pd, Pt, Ru, Au, Os, Ir, La. Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu. The scheme shows two routes, sharing maleimide as a common precursor. One route was based on the modified Barton-Zard synthesis of sulfolenolpyrrole (a method of pyrrole synthesis by a cyclization reaction between a nitroalkene and α-isocyanoacetate under base conditions) developed previously by Vicente et al., Tetrahedron Letters 38:3639-3642 (1997). A second route was also feasible; however, conditions of the Barton-Zard reaction (Barton, Zard, “A new synthesis of pyrroles from nitroalkenes,” J. Chem. Soc. 1098 (1985)), needed to be adjusted for each specific case, as its outcome is likely to be affected by the presence of aromatic imide group. The stability of this imide depends on the substituents R and their positions (given that electron-withdrawing substituents in 3, 5-positions will de-stabilize the imide with respect to hydrolytic cleavage). Accordingly, to insure better protection of meso-unsubstituted porphyrins already at early dendritic generations in at least one embodiment, 2,6-substituents were used, which direct the dendrons under and above the porphyrin plane.

In one embodiment of the invention, the TAPIP and DAMP porphyrins depicted in FIG. 2 are the products of the synthesis schemes shown in FIG. 3 and FIG. 4, with M being selected from H₂, Zn, Ni, CU, Pd, Pt, Ru, Au, Os, Ir, La. Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu.

FIG. 3 depicts TAPIP synthesis, which starts with the Barton-Zard-type reaction of sulfolene 1, bearing an electro-withdrawing group X (e.g. NO₂ of SO₂Ar), with isocyanoacetate to give sulfolenolpyrrole ester 4. Although FIG. 3 depicts X as being NO2, the invention is not so limited, and with the benefit of the present disclosure, one skilled in the art would be enabled to begin the synthesis with a sulfolene having any electro-withdrawing group at this position. In parallel maleimide 3 is synthesized from maleic anhydride 2 and amine R—NH₂, where group R is an aryl or an akyl, and is selected from the group comprising methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, decyl, dodecyl, phenyl, tolyl, xylyl, hydroxyphenyl, dihydroxyphenyl, aminophenyl, sulfophenyl, and bromophenyl. In a preferred embodiment, as depicted in FIG. 2, the groups R are 2,6-disubstituted aryl groups, as these are advantageous for their high solubility. Because of steric hindrance caused by two substituents R₂, the 2,6-disubstituted aryl group rotates out of plane of the pyrrole ring in sulfolenolpyrrole 4 as well as in all subsequent structures. This out-of-plane geometry prevents aggregation and increases solubility of the target porphyrins.

Diels-Alder reaction of sulfolenopyrrole ester 4 and maleimide 3 generates cyclohexenopyrrole ester 5, which upon cleavage of ester groups gives pyrrole 6. Pyrrole 6 is then introduced into the reaction with formaldehyde in the presence of an acidic catalyst, followed by oxidation, generating tetracyclohexenoporphyrin 7. In a preferred embodiment, the acidic catalyst is trifluoroacetic acid. This porphyrin may be metallated using a variety of metal salts, with salts containing metal M selected from Zn, Ni, Cu, Pd, Pt, Ru, Au, Os, Ir, La, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu being particularly useful for gaining useful luminescent and photodynamic properties. The resulting metalloporphyrin is oxidized into the metallo-TAPIP (9), using oxidants such as dichlorodicyanobenzoquinone (DDQ) or its analogues. In an alternative pathway, a free-base version of tetracyclohexenoporphyrin 7 can be oxidized into TAPIP free-base (9a) and then metallated with a metallic salt having metal M, wherein metal M is selected from the group comprising Zn, Ni, Cu, Pd, Pt, Ru, Au, Os, Ir, La, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu, to produce a metalloporphyrin.

FIG. 4 depicts a similar synthesis scheme to be applied for the purpose of synthesizing DAPIP rather than TAPIP. The first steps of this synthesis are the same as those in the synthesis of TAPIP, and are incorporated herein by reference; however after assembling pyrrole ester 5, instead of ester cleavage/decarboxylation, pyrrole ester 5 is introduced into reaction with itself to give dipyrromethane-diester 10. Dipyrromethane-diester 10 is then de-esterified, decarboxylated and condensed with diformyldipyrromethane 11. Syntheses of dipyrromethanes 11 are well-developed and known from the literature, and substituents R1 and R2 can vary between different alkyl and aryl groups. In a preferred embodiment, where R1=R2=H, dipyrromethane 11 is unsubstituted diformyl-dipyrromethane, which can be generated in bulk quantities by reaction of pyrrole with formaldehyde in excess pyrrole used as a solvent, followed by formylation into α-positions. Importantly, groups Cl are formyl groups, synthons of the same, or any groups exhibiting the same formal reactivity as formyl groups and yielding the same products; in any case the groups Cl yield formyl groups in situ during the acid-catalyzed reaction with diformyldipyrromethane 11.

In one embodiment, the group R of amines R—NH2 are 2,6-disubstituted aryl groups, as these are advantageous for their high solubility.

The subsequent reactions—metallation followed by oxidation or vice versa—exactly replicate those in the synthesis of TAPIP depicted in FIG. 3. Just as with TAPIP, there is an alternative pathway in which a free-base version of dicyclohexenoporphyrin is oxidized to yield DAPIP free-base. This DAPIP free-base is then, in turn, metallated with a metallic salt having metal M, wherein metal M is selected from the group comprising Zn, Ni, Cu, Pd, Pt, Ru, Au, Os, Ir, La, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu, to produce a metalloporphyrin.

B) Luminescence of Meso-Unsubstituted Phthalimidoporphyrins.

Metal complexes of TAPIP and DAPIP with 2,6-disubstituted aryl groups R are well-soluble in organic solvents. These metalloporphyrins have strong absorption in the visible/near infrared regions of the spectrum. Pt and Pd complexes phosphoresce at ambient temperature with very high quantum yields (from 0.4 to 0.45 at 22 degrees Celsius). The phosphorescence quantum yields reach 0.45 in organic solvents, such as dimethylformamide, at 22 degrees Celsius—a rare and useful property for applications. Zn and other lighter metal complexes fluorescence. FIGS. 7A-7H depict the absorption and emission spectra, whether phosphorescence or fluorescence, of Zn, Pd and Pt complexes of DAPIP and TAPIP: FIG. 5A shows the absorption spectra of ZnTAPIP; FIG. 5B shows the fluorescence of ZnTAPIP; FIG. 5C shows the absorption spectra of PdTAPIP; FIG. 5D shows the phosphorescence of PdTAPIP; FIG. 5E shows the absorption spectra of PtTAPIP; FIG. 5F shows the phosphorescence of PtTAPIP; FIG. 5G shows the absorption of PtDAPIP: FIG. 5H shows the phosphorescence of PtDAPIP.

Bright phosphorescence makes Pt and Pd complexes of DAMP and TAPIP very valuable as core chromophores for oxygen sensing based on phosphorescence quenching.

C) Improved Procedure for Dendrimerization of Porphyrins.

Embodiments of the invention have shown that attachment of extension linkers to the anchor groups on either meso-aryl rings or directly on porphyrin macrocycle greatly facilitates coupling of the protecting dendrons. Specifically, extension of carboxylic groups with γ-aminobutyrate linkages (“extension arms”) permitted high yield synthesis of monodisperse dendritic oxygen probes or improved sensitivity and higher purity (See, basic photophysical studies as a foundation for determining the significantly higher phosphorescence quantum yields of the 5,15-diaryl-substituted π-extended porphyrins, as compared with tetraarylporphyrins by Esipova et al., “Two new “protected” oxyphors for biological oximetry: properties and application in tumor imaging,” Analytical Chem. 83:8756 (published on-line Oct. 11, 2011).

Dendrimerization of phosphorescent porphyrins includes hydrolysis of the peripheral ester groups on the porphyrin, attachment of dendrons, hydrolysis of their peripheral esters on the dendrons and PEGylation of the resulting free carboxyl groups. See, FIG. 1. These methods have been developed by the inventors and described in their previous patents cited above, and incorporated herein by reference. One critical improvement, however, that was only recently established, relates to the yield and purity-limiting step in the synthesis—that is, attachment of the bulky dendritic substituents to the porphyrin core. This step typically proceeds via one of the standard peptide coupling reactions, or any other suitable chemistry. Yet the steric hindrance imposed by large folded dendritic groups impedes the reaction. However, if the anchor groups are extended by flexible linkers, bulky substrate react slowly because of unfavorable steric reasons, and thus the actual reaction sites are placed at a larger distance from one-another, they become much more accessible to nucleophilic attack. Consequently, the resulting reaction occurs with higher rate, i.e. complete dendrimerization is reached overnight (approx. 24 hours), as opposed to 7 days in the case of porphyrins without extension arms, and provides clean octa-dendrimerized porphyrin, as opposed to mixture of hexa-, hepta- and octa-dendrimerized porphyrins (imperfect contaminating dendrimers) that were obtained in the case of porphyrins without extension arms.

The overall scheme of the synthesis is shown in FIG. 7 for the case of 5,15-diaryl-p-extended porphyrins (vide supra), with M being selected from H₂, Zn, Ni, CU, Pd, Pt, Ru, Au, Os, Ir, La. Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu. The extension step is the first step in the reaction sequence, and the addition of AG3 elements (third generation (Gen 3)) arylglycine dendrimers.

D) Increase in the Excitation Cross-Sections of the Probe Via Intramolecular Fluorescence Resonance Energy Transfer (FRET).

One approach to enhancing production of excitement cross-sections in metalloporphyrins without directly altering their electronic properties involves harvesting the excitation energy by an electronically separate antenna and to pass it onto the phosphorescent core via intramolecular Förster-type resonance energy transfer (FRET) (See, Briñas et al., J. Amer. Chem. Soc. 127:11851 (2005)). In such an antenna-core system constructed around a dendrimer, the latter regulates the rate of oxygen diffusion to the core, just as in the regular dendritic probes (see above), while the dendrimer termini control the probe bio-distribution.

Resonance energy transfer is the radiationless transmission of an energy quantum from its site of absorption to the site of its utilization in the molecule, or system of molecules, by resonance interaction between chromophores, over distances considerably greater than interatomic distance, without conversion to thermal energy, and without the donor and acceptor coming into kinetic collision. The donor is the marker that initially absorbs the energy, and the acceptor is the chromophore to which the energy is subsequently transferred. (from Van Der Meer, Coker, and Chen, Resonance Energy Transfer Theory and Data, VCH, New York, 1994).

Förster (Fluorescence) resonance energy transfer (FRET), resonance energy transfer (RET) or electronic energy transfer (EET), is a mechanism describing energy transfer between two chromophores. [1] A donor chromophore, initially in its electronic excited state, may transfer energy to an acceptor chromophore through nonradiative dipole-dipole coupling. [2] The efficiency of this energy transfer is inversely proportional to the sixth power of the distance between donor and acceptor making FRET extremely sensitive to small distances. [3] Measurements of FRET efficiency can be used to determine if two fluorophores are within a certain distance of each other. [4] Such measurements are used as a research tool in fields including biology and chemistry. When both chromophores are fluorescent, the term “fluorescence resonance energy transfer” is often preferred, although the energy is not actually transferred by fluorescence. In order to avoid an erroneous interpretation of the phenomenon that is always a nonradiative transfer of energy (even when occurring between two fluorescent chromophores.

FRET is analogous to near field communication, in that the radius of interaction is much smaller than the wavelength of light emitted. In the near field region, the excited chromophore emits a virtual photon that is instantly absorbed by a receiving chromophore. These virtual photons are undetectable, since their existence violates the conservation of energy and momentum, and hence FRET is known as a radiationless mechanism. Quantum electrodynamical calculations have been used to determine that radiationless (FRET) and radiative energy transfer are the short- and long-range asymptotes of a single unified mechanism. Jablonski diagrams illustrate the electronic states of a molecule and the transitions between them. The states are arranged vertically by energy and grouped horizontally by spin multiplicity (Jablonski, Aleksander “Efficiency of Anti-Stokes Fluorescence in Dyes” Nature 131:839-840 (1933)).

1) Theoretical Basis of FRET:

When the donor probe is a fluorescent molecule, and when light excites the fluorophore at an appropriate wavelength (250-500 nm), its electrons jump from the ground state (S) to a higher vibrational level (S, S₀, S₁, etc). Within picoseconds these electrons decay to the lowest of these vibrational levels (S) and then decay more slowly (nsec) to one of the S states and a photon of light is emitted whose wavelength is longer than that of the exciting wavelength. The acceptor probe can be fluorescent or non-fluorescent.

The FRET efficiency depends on many physical parameters that can be grouped as follows:

-   -   The donor probe must have a high quantum yield.     -   The spectral overlap of the donor emission spectrum and the         acceptor absorption spectrum. The emission spectrum of the donor         probe must overlap considerably the absorption spectrum of the         acceptor probe (overlap integral).     -   There is an appropriate alignment of the absorption and emission         moments and their separation vector (embodied in kappa square).     -   The distance between the donor and the acceptor. The donor and         acceptor must be within 1±0.5×r_(o) from each other, when         r=donor-to-acceptor separation distance.     -   The relative orientation of the donor emission dipole moment and         the acceptor absorption dipole moment.

Accordingly, FRET efficiency relates to the quantum yield and the fluorescence lifetime of the donor molecule as follows (See, e.g., Majoul et al. (2006). “Practical Fluorescence Resonance Energy Transfer or Molecular Nanobioscopy of Living Cells.” In Pawley, Handbook Of Biological Confocal Microscopy (3rd ed.). New York, N.Y.: Springer. pp. 788-808). In fluorescence microscopy, fluorescence confocal laser scanning microscopy, as well as in molecular biology, FRET is a useful tool to quantify molecular dynamics in biophysics and biochemistry, such as protein-protein interactions, protein—DNA interactions, and protein conformational changes. For monitoring the complex formation between two molecules, one is labeled with a donor, and the other with an acceptor. The FRET efficiency is measured and used to identify interactions between the labeled complexes. After excitation, the states of the antenna (^(a)S_(2P)) are populated and have internally converted into the lowest excited singlet state ^(a)S₁, the excess energy is transferred to the core.

The Förster energy transfer mechanism assumes that the fluorescence (^(a)S₁→^(a)S₀) of the donor (2P antenna) overlaps with an absorption band ^(c)S_(n)←^(c)S₀ (n=1, 2 . . . ) of the acceptor (core). Therefore, the core must possess linear absorption band(s) somewhere in the region extending to the red from 400 nm. Exact positions of these bands are defined by the Stokes shift of the fluorescence of the antenna relative to its absorption at 400 nm. The FRET from the antenna to the core results either in the population of its singlet excited state ^(c)S₁, which is depopulated via the intersystem crossing (“isc”) to yield the triplet state ^(c)T₁, resulting in either oxygen quenching or phosphorescence. Thus, FRET efficiency is the quantum yield of the energy transfer transition, i.e., the fraction of energy transfer event occurring per donor excitation event. There are several ways of measuring the FRET efficiency by monitoring changes in the fluorescence emitted by the donor or the acceptor or as the variation in acceptor emission intensity (Clegg, R. (2009). In Gadella, Theodorus, FRET and FLIM Techniques. Laboratory Techniques in Biochemistry and Molecular Biology, Vol. 33, Elsevier. pp. 1-57). When the donor and acceptor are in proximity (1-10 nm) due to the interaction of the two molecules, the acceptor emission increases because of the intermolecular FRET from the donor to the acceptor.

E) Two-Photon Absorption of Meso-Unsubstituted Phthalimidoporphyrins.

DAMP and TAPIP have uniquely strong two-photon absorption in the region of 800-1000 nm. PtTAPIP has two-photon absorption (2PA) cross-section near 950 nm of ˜500 Goppert-Mayer (GM) units. FIG. 6 depicts the 2PA spectra of PtTAPIP and PdTAPIP. Metal complexes of TAPIP, e.g. PtTAPIP and PdTAPIP, belong to the D_(4h) symmetry class. Therefore, their ground and excited states have definite parity: either gerade or ungerade states. In D_(4h) and other systems with inversion of symmetry, the selection rules governing electric-dipole transitions by one-photon (1P) or two-photon (2P) mechanisms are mutually exclusive. For 1P absorption, transitions from the ground state (g-state) are allowed only into u-states. For 2P absorption, transitions from the ground state are allowed only to g-states. Typically, in porphyrins 2P-allowed states (g-states) lie at high energies, such that excitation at half that energy (which is required for 2P absorption) overlaps with low-lying vibronic bands of 1P allowed states. As a result, 2P absorption is overshadowed by 1P absorption into the 1P vibronic states. Furthermore, in Pt and Pd porphyrins, due to the very strong spin-orbit coupling, direct spin-forbidden absorption into the triplet state (S0→T1) gains non-negligible dipole strength. Consequently, 2P excitation in regular Pt and Pd porphyrins becomes impossible, as energies below the triplet state level are insufficient to promote 2P absorption into higher-lying g-states.

In DAPIP and TAPIP, g-states are stabilized below the B-state level, where B-state is the second strongly allowed excited state, also known as Soret state. For example, Pt and Pd TAPIP have strongly 2P-allowed g-symmetry states near 450 nm (or ˜900 nm for 2P excitation, as shown in FIG. 6). As a result, very efficient excitation into these states becomes possible, since there is no 1P absorption into the triplet state or the singlet Q-state that interferes with 2P excitation at ˜900 nm. Because of their unique positioning of 2P-allowed g-states, combined with strong ability to form triplet states, TAPIP and DAPIP present interest for two-photon phosphorescence lifetime microscopy (2PLM).

F) Dendritic Phosphorescent Probes are Suitable for Oxygen Measurements in Liquid Organic Media, e.g., Organic Solvents or Oils.

The present invention provides oxygen sensors that can be designed to be dissolved in water media (for use in biological systems) or designed to be dissolved in organic media (for use in specialized oxygen sensors for any process in which organic media can be used, including those requiring organic media. This is a specific section for those that would best be dissolved in organic media, for which the external shell would need to different from those used in water based media. To achieve solubility of the dendritic probes in organic media the termini of the dendrimers (e.g., carboxyl groups) are amidated using 1-aminoalkanes, or esterified using 1-hydroxyalkanes to create a supramolecular hydrophobic outer layer (FIG. 8, wherein M is selected from H₂, Zn, Ni, CU, Pd, Pt, Ru, Au, Os, Ir, La. Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu). The chemistry for this modification and the purification protocols closely resembles the above-discussed procedures for covering dendrimer surfaces with PEG groups. But in accordance with addition of the supermolecular hydrophobic outer layer, the resulting probes showed extremely high solubility in saturated hydrocarbons, aromatic mineral oils and other organic solvents, whereas without attachment of the new outermost layer the probe remains completely insoluble in such liquids.

In order to keep the Stern-Volmer oxygen quenching constant of the probe suitable for oxygen measurements in the physiological pO₂ range, polyarylglycine or other polyamide dendrimers (namely, polyglutamic, polyesteramide, polyarylamide) have been tested. These dendrimers fold well in aqueous, as well as in organic environments, serving to attenuate oxygen access to the phosphorescent cores. Thus, essentially the same dendrimers can be used for both aqueous and hydrophobic environments, and only the outer layers (“supramolecular”) needs to be changed.

In sum, methods are provided for substantially improving the currently available oxygen sensitive phosphors by increasing the quantum efficiency (phosphorescence intensity) and extending their range of applicability through making a class of oxygen sensors for measurements in organic media. Thus, methods are provided in the present invention for synthesizing new porphyrin constructs in which the porphyrin is made less flexible and more planar, changing with decrease internal quenching and thereby increasing the phosphorescence emission used for oxygen sensing. Additional methods are provided for structurally modifying the dendrimer used to encapsulate the porphyrin phosphor to provide for internal quenching of any singlet oxygen formed while measuring oxygen. Moreover, in the present invention it is the outer layer that controls the solubility of the probe as a whole. If the probe needs to be soluble in water—a water-soluble outer layer is added; whereas if the probe needs to be soluble in organic media—an outer layer is added, making it compatible with organics. The inventors' experiments have shown that Pd and Pt porphyrin-based Gen 2 arylglycine dendrimers (AG2), modified at the periphery with 1-hexadecylamine possess high (ca millimolar) solubility in a variety of organic solvents (e.g., oils, saturated hydrocarbons, aromatic mineral oils, benzene, toluene, hexane, octane, tetrahydrofurane, saturated, alkanes, mineral oil, cooking oils, oils used in food or cosmetics, and organic liquids used in tissue and biological analyses, and any equivalent thereof), permitting phosphorescence measurements throughout the entire ambient oxygen range: pO₂=0-160 mm Hg.

The disclosure of each patent, patent application and publication cited or described in this document is hereby incorporated herein by reference, in its entirety.

While the foregoing specification has been described with regard to certain preferred embodiments, and many details have been set forth for the purpose of illustration, it will be apparent to those skilled in the art without departing from the spirit and scope of the invention, that the invention may be subject to various modifications and additional embodiments, and that certain of the details described herein can be varied considerably without departing from the basic principles of the invention. Such modifications and additional embodiments are also intended to fall within the scope of the appended claims. 

What we claim is:
 1. A phosphorescent metalloporphyrin probe, also referred to as a dendritic oxygen probe, effective for oxygen measurement in human or animal tissue, said dendritic oxygen probe comprising a meso-unsubstituted, metallo-tetrabenzoporphyrin core, wherein the metal M is Pt, and the metallo-tetrabenzoporphyrin core has the following structure:

a dendrimer comprising dendrons, wherein the dendrons are peripherally attached to the metallo-tetrabenzoporphyrin core at the 2,6 positions indicated by “R”; and a solubilizing layer attached to the periphery of the dendrons.
 2. The phosphorescent probe of claim 1, wherein the solubilizing layer is a polyethyleneglycol (PEG) layer.
 3. The phosphorescent probe of claim 1, wherein the solubilizing layer is a hydrocarbon layer.
 4. A method of using the metalloporphyrin probe of claim 1, the method comprising the steps of: dissolving the probe in the blood, and exciting the probe using appropriate illumination, wherein the probe exhibits strong light absorption in a near infrared region of a spectrum and upon excitation, provides quantum yields of phosphorescence 5-10 fold higher, as compared with a corresponding tetraarylporphyrin when measured at the same temperature and conditions.
 5. A method of improving dendrimerization of a meso-unsubstituted, metallo-tetrabenzoporphyrin core, wherein the metal M is Pt, and the metallo-tetrabenzoporphyrin core has the following structure

wherein “R” indicates the attachment of dendrons to the core at 2, 6 positions, the method comprising the steps of: attaching flexible extension linkers terminated by functional groups to functional groups positioned directly on the metallo-tetrabenzoporphyrin core, and thereby spacing reaction sites at a sufficient distance apart to cause enhancing of nucleophilic attack and reduce contamination by imperfect dendrimers in a yield and purity enhancing step.
 6. A method of using the improved dendrimerization method of claim 5 using a metalloporphyrin probe, wherein the attachment of the flexible extension linkers provides 1-2 times higher-yield of synthesis of pure monodisperse dendritic oxygen probes as compared to corresponding phosphorescent porphyrins synthesized by the same steps of hydrolysis of peripheral ester groups, attachment of dendrons and hydrolysis of their peripheral esters and PEGylation, but without attaching flexible extension linkers to anchor groups during synthesis at the same temperature and conditions.
 7. A phosphorescent metalloporphyrin probe having improved dendrimerization, also referred to as a dendritic oxygen probe, effective for oxygen measurement in human or animal tissue, said dendritic oxygen probe produced by the method of claim 5, the probe comprising added flexible extension linkers attached to anchor groups on either meso-aryl rings or directly on a metalloporphyrin macrocycle, thereby spacing reaction sites at a sufficient distance apart to enhance nucleophilic attack and reduce contamination by imperfectly reacted dendrimers after a reaction time of only the overnight period at room temperature.
 8. A method of causing a dendritic phosphorescent probe suitable for oxygen measurements in aqueous liquids, the method comprising: adding a three dimensional supramolecular hydrophilic outer layer to the termini of a dendrimer having a meso-unsubstituted, metallo-tetrabenzoporphyrin core, wherein the metal M is Pt, and the metallo-tetrabenzoporphyrin core has the following structure:

wherein “R” indicates the attachment of dendrons to the core at 2, 6 positions.
 9. A method of causing a dendritic phosphorescent probe suitable for oxygen measurements in organic liquids, the method comprising: adding a three dimensional supramolecular hydrophobic outer layer to the termini of hydrophobic dendrimers having a meso-unsubstituted, metallo-tetrabenzoporphyrin core, wherein the metal M is Pt, and the metallo-tetrabenzoporphyrin core has the following structure:

wherein “R” indicates the attachment of dendrons to the core at 2, 6 positions; causing the molecule to remain folded, but to become highly soluble in organic solvents selected from the group comprising oils, saturated hydrocarbons, mineral oil and aromatic mineral oils, benzene, saturated alkanes, tetrahydrofuran (THF), toluene, hexane, octane, cooking oils, oils used in food or cosmetics, and organic liquids used in tissue and biological analyses; and enabling oxygen measurements therein.
 10. A dendritic phosphorescent probe produced by the method of claim 9, comprising a selectably added three dimensional supramolecular hydrophobic outer layer attached to the termini of the hydrophobic dendrimers, thereby causing the molecule to remain folded, and to be highly soluble in organic solvents selected from the group comprising oils, saturated hydrocarbons, mineral oil and aromatic mineral oils, benzene, saturated alkanes, tetrahydrofuran (THF), toluene, hexane, octane, cooking oils, oils used in food or cosmetics, and organic liquids used in tissue and biological analyses. 